@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP55021.RAW2xUDu0oDieb5WWbxzqtvs_Ad3ljXJ0VosQBpWGKf0I
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP55021.RAW2xUDu0oDieb5WWbxzqtvs_Ad3ljXJ0VosQBpWGKf0I130_head
{
this:
np:hasAssertion
dgn-np:NP55021.RAW2xUDu0oDieb5WWbxzqtvs_Ad3ljXJ0VosQBpWGKf0I130_assertion
;
np:hasProvenance
dgn-np:NP55021.RAW2xUDu0oDieb5WWbxzqtvs_Ad3ljXJ0VosQBpWGKf0I130_provenance
;
np:hasPublicationInfo
dgn-np:NP55021.RAW2xUDu0oDieb5WWbxzqtvs_Ad3ljXJ0VosQBpWGKf0I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP55021.RAW2xUDu0oDieb5WWbxzqtvs_Ad3ljXJ0VosQBpWGKf0I130_assertion
a
np:Assertion
.
dgn-np:NP55021.RAW2xUDu0oDieb5WWbxzqtvs_Ad3ljXJ0VosQBpWGKf0I130_provenance
a
np:Provenance
.
dgn-np:NP55021.RAW2xUDu0oDieb5WWbxzqtvs_Ad3ljXJ0VosQBpWGKf0I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP55021.RAW2xUDu0oDieb5WWbxzqtvs_Ad3ljXJ0VosQBpWGKf0I130_assertion
{
miriam-gene:4128
a
ncit:C16612
.
lld:C0019337
a
ncit:C7057
.
dgn-gda:DGNb457b5016da7f03a73aa034efc728719
sio:SIO_000628
miriam-gene:4128
,
lld:C0019337
;
a
sio:SIO_001122
.
}
dgn-np:NP55021.RAW2xUDu0oDieb5WWbxzqtvs_Ad3ljXJ0VosQBpWGKf0I130_provenance
{
dgn-np:NP55021.RAW2xUDu0oDieb5WWbxzqtvs_Ad3ljXJ0VosQBpWGKf0I130_assertion
dcterms:description
"[The long-repeat allelic variants (>4-repeats) and 2-repeat allele of the DRD4 exon 3 VNTR polymorphism might be risk alleles for individual vulnerability to heroin addiction in Chinese men, but the MAOA promoter VNTR polymorphism does not mean that the partial dominant inherited mode might involved in the genetics of heroin dependence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:20218801
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP55021.RAW2xUDu0oDieb5WWbxzqtvs_Ad3ljXJ0VosQBpWGKf0I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:25+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}